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- An attempt to prepare sulfonyl analogues of fotemustine: unexpected rearrangement to sulfamate during nitrosation step. Zineb Aouf, Sara Boughaba, Rayene Sayad, Jacques Lebreton, Monique Mathe-Allainmat, Nour-Eddine Aouf
, RSC Adv.
, 2023
, 13
, 35741
- Nucleoside analogues. Part 2. Further molecular combinations of (5-substituted) uracil and N-(2-chloroethyl)-N-nitrosourea residues as anticancer agents. Joan E. McCormick, R. Stanley McElhinney
, J. Chem. Soc., Perkin Trans. 1
, 1985
, 93
- Flow synthesis kinetics for lomustine, an anti-cancer active pharmaceutical ingredient. Samir Diab, Mateen Raiyat, Dimitrios I. Gerogiorgis
, React. Chem. Eng.
, 2021
, 6
, 1819
- Formation of N-tributylstannyl-2-oxazolidone from (Bu3Sn)2O and 2-chloroethyl isocyanate. Ikuya Shibata, Akio Baba, Haruo Matsuda
, J. Chem. Soc., Chem. Commun.
, 1986
, 1703
- Nitric oxide release by N-(2-chloroethyl)-N-nitrosoureas: a rarely discussed mechanistic path towards their anticancer activity. Amrita Sarkar, Subhendu Karmakar, Sudipta Bhattacharyya, Kallol Purkait, Arindam Mukherjee
, RSC Adv.
, 2015
, 5
, 2137
- A restricted access molecularly imprinted polymer coating on metal–organic frameworks for solid-phase extraction of ofloxacin and enrofloxacin from bovine serum. Zhian Sun, Huachun Liu, Yanqiang Zhou, Shanwen Zhao, Jianmin Li, Xiaoxiao Wang, Bolin Gong
, RSC Adv.
, 2019
, 9
, 27953
- Disulfide bonds-containing amphiphilic conetworks with tunable reductive-cleavage. Shan Zhang, Heng Chen, Jie Kong
, RSC Adv.
, 2016
, 6
, 36568
- Utilizing tautomerization of 2-amino-oxazoline in hydrogen bonding tripodal ligands. Young Jun Park, Nathaniel S. Sickerman, Joseph W. Ziller, A. S. Borovik
, Chem. Commun.
, 2010
, 46
, 2584
- Polyvalent DNA–graphene
nanosheets “click” conjugates. Zihao Wang, Zhilei Ge, Xiaoxue Zheng, Nan Chen, Cheng Peng, Chunhai Fan, Qing Huang
, Nanoscale
, 2012
, 4
, 394
- A novel single-fluorophore-based ratiometric fluorescent probe for direct detection of isocyanates in air. Zhenzhong Gao, Baichuan Han, Kai Chen, Jin Sun, Xianfeng Hou
, Chem. Commun.
, 2017
, 53
, 6231